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BMS (BMY)-Pfizer (PFE) Alliance to Unveil Real-World Data Analyses Associated with Oral Anticoagulants in NVAF
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BMS-Pfizer Alliance to Unveil Real-World Data Analyses - Cost, Safety and Comparative Effectiveness Findings Associated with Oral Anticoagulants in Non-Valvular Atrial Fibrillation
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Bristol-Myers Squibb (BMY) Says Encouraging Response Observed with Opdivo Plus Investigational IDO1 Inhibitor, BMS-986205, in Heavily Pre-Treated Patients with Advanced Cancers in Phase 1/2a Study CA0
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Encouraging Response Observed with Opdivo (nivolumab) Plus Investigational IDO1 Inhibitor, BMS-986205, in Heavily Pre-Treated Patients with Advanced Cancers in Phase 1/2a Study CA017-003
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Bristol-Myers Squibb (BMY) Announces FDA Expanded Approval for Sprycel to Include Children with Ph+ CML in Chronic Phase
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U.S. Food and Drug Administration Expands Approval of Sprycel® (dasatinib) to Include Treatment of Children with Philadelphia Chromosome-Positive Chronic Myeloid Leukemia in Chronic Phase
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Bristol-Myers Squibb (BMY) & Five Prime (FPRX) Announce Phase 1a/1b Data Evaluating Cabiralizumab (anti-CSF-1 receptor antibody) with Opdivo (nivolumab) in Patients with Advanced Solid Tumors
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Bristol-Myers Squibb and Five Prime Present Phase 1a/1b Data Evaluating Cabiralizumab (anti-CSF-1 receptor antibody) with Opdivo (nivolumab) in Patients with Advanced Solid Tumors
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Bristol-Myers Squibb to Take Part in Jefferies London Healthcare Conference
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Opdivo Plus Yervoy Combination Delivered Overall Survival Benefit Across PD-L1 Expression Levels in Intermediate- and Poor-Risk Patients with Previously Untreated Advanced or Metastatic Renal Cell Car
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Bristol-Myers Squibb (BMY) to Highlight Clinical and Translational Research at SITC
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Bristol-Myers Squibb to Highlight Clinical and Translational Research at the Society for Immunotherapy of Cancer (SITC) 32nd Annual Meeting
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Opdivo (nivolumab) Demonstrates Superior Three-Year Survival Benefit for Patients with Previously Treated Advanced Renal Cell Carcinoma (RCC)
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Bristol-Myers Squibb (BMY) to Showcase Progress in Researching Personalized Medicine for Potential Treatment of Autoimmune Diseases at ACR/ARHP Meeting
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Bristol-Myers Squibb to Showcase Company’s Progress in Researching Personalized Medicine for the Potential Treatment of Autoimmune Diseases at 2017 American College of Rheumatology and Association o
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Bristol-Myers Squibb, BioLabs Announce Founding Sponsorship in Support of Promising Biotech Companies in New York
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Bristol-Myers Squibb (BMY) Reports EMA Validates Type II Variation Application for Opdivo (Nivolumab)
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European Medicines Agency Validates Bristol-Myers Squibb’s Type II Variation Application for Opdivo (nivolumab) for Treatment of Patients with Resected High-Risk Advanced Melanoma
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Bristol-Myers Squibb Reports Third Quarter Financial Results
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Dow, S&P gain but Nasdaq dips as healthcare lags
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Bristol-Myers Squibb to Present New Data Advancing Research Across Serious Liver Diseases at The Liver Meeting® 2017
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Bristol-Myers Squibb (BMY) Says FDA Accepted its Application for Opdivo in Patients with Resected High-Risk Advanced Melanoma and Grants Priority Review
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U.S. Food and Drug Administration (FDA) Accepts Bristol-Myers Squibb’s Application for Opdivo (nivolumab) in Patients with Resected High-Risk Advanced Melanoma and Grants Priority Review
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Opdivo Alone or Combined with Yervoy Shows Encouraging Response and Survival Rates in Recurrent Small Cell Lung Cancer Patients with High Tumor Mutation Burden, in Exploratory Analysis from Phase 1/2
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Bristol-Myers Squibb Appoints Saurabh Saha, M.D., Ph.D., as Senior Vice President, Global Head of Translational Medicine
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Caregivers Wish Liver Cancer Received Greater Public Awareness in the U.S., New Survey Reveals
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Bristol-Myers Squibb (BMY) Announces Presentations at IASLC
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Bristol-Myers Squibb: Advancing Research Across Thoracic Cancers with New Data at IASLC 18th World Conference on Lung Cancer
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Bristol-Myers Squibb (BMY) Granted FDA Approval for Opdivo for Treatment of Hepatocellular Carcinoma Patients
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Bristol-Myers Squibb’s Opdivo® (nivolumab) Receives FDA Approval for the Treatment of Hepatocellular Carcinoma Patients Previously Treated with Sorafenib
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AbbVie (ABBV), Bristol-Myers Squibb (BMY) Announce Pact to Evaluate Therapeutic Regimen in Advanced Solid Tumors
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AbbVie and Bristol-Myers Squibb Announce Clinical Research Collaboration to Evaluate a Therapeutic Regimen in Advanced Solid Tumors
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AbbVie and Bristol-Myers Squibb Announce Clinical Research Collaboration to Evaluate a Therapeutic Regimen in Advanced Solid Tumors
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Bristol-Myers Squibb (BMY) Granted Approval by Japanese Ministry of Health for Opdivo (nivolumab) Based on 3 Study ATTRACTION-2 (ONO-4538-12)
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Japan Ministry of Health, Labor and Welfare Approves Opdivo (nivolumab) for the Treatment of Patients with Unresectable Advanced or Recurrent Gastric Cancer Which Has Progressed After Chemotherapy
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Bristol-Myers Squibb to Take Part in Leerink Partners Rare Disease & Immuno-Oncology Roundtable Conference
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New Global Report Finds Majority of People at High Risk of Stroke Not Being Screened for Common Risk Factors
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Bristol-Myers Squibb (BMY), Halozyme (HALO) Enter Pact for ENHANZE Technology
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Bristol-Myers Squibb and Halozyme Enter Global Collaboration and License Agreement for ENHANZE Technology
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Bristol-Myers Squibb Announces Dividend
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Bristol-Myers Squibb (BMY) Names Karen Vousden to Board of Directors
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Bristol-Myers Squibb Names Karen Vousden, Ph.D. to Board of Directors
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Bristol-Myers Squibb (BMY) Reports Opdivo (nivolumab) Demonstrates Superior Recurrence-Free Survival Versus Yervoy (ipilimumab) in Phase 3 CheckMate -238 Study
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Bristol-Myers Squibb (BMY) Reports Opdivo Plus Yervoy Combination Demonstrated Superior Overall Survival in Phase 3 CheckMate -214 Trial
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Opdivo (nivolumab) Demonstrates Superior Recurrence-Free Survival Versus Yervoy (ipilimumab) for Patients with Resected High-Risk Melanoma in Phase 3 CheckMate -238 Study
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Opdivo Plus Yervoy Combination Demonstrated Superior Overall Survival and Showed Durable Responses in Patients with Previously Untreated Advanced or Metastatic Renal Cell Carcinoma in Phase 3 CheckMat
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Bristol-Myers Squibb (BMY) Reports Two Pivotal Opdivo (nivolumab) Trials Show Three-Year Survival Benefit in Patients with Previously Treated Advanced Non-Small Cell Lung Cancer
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Two Pivotal Opdivo (nivolumab) Trials Show Three-Year Survival Benefit in Patients with Previously Treated Advanced Non-Small Cell Lung Cancer
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Bristol-Myers Squibb Completes Previously Announced Acquisition of IFM Therapeutics
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Bristol-Myers Squibb (BMY) Reports CheckMate-214 Study Evaluating Opdivo in Combination with Yervoy Meets Co-Primary Endpoint, Demonstrating Superior Overall Survival Compared to Sunitinib

